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1.
Long chain 1,14-diols and 12-hydroxy methyl alkanoates are biomarker lipids for Proboscia diatoms and occur widely in Quaternary sediments. To determine the effect of temperature on the lipid composition of these algae, a new Proboscia sp. culture grown at 8 °C and Proboscia indica cultures grown at 18, 21, 24 and 27 °C were examined. The results were combined with lipid data from a P. indica culture and a Proboscia alata culture, grown at 20 and 2 °C, respectively, from previous studies. The data showed a strong relationship between long chain diol and 12-hydroxy methyl alkanoate composition and growth temperature, i.e. the chain length increases and the degree of unsaturation of long chain 1,14-diols decreases with increasing growth temperature. To determine the effect of temperature on Proboscia lipid compositions in natural environments, we also analyzed fossil long chain 1,14-diols and 12-hydroxy methyl alkanoates in surface sediments derived from Proboscia diatoms living in the water column of the eastern South Atlantic. The results indicate a significant relationship between sea surface temperature and chain length distribution of saturated long chain diols, but also suggest that the relative abundances of unsaturated long chain diols and 12-hydroxy methyl alkanoates in sediments are predominantly determined by factors other than temperature.  相似文献   

2.
Long chain 1,14-diols have been reported in diatoms of the genus Proboscia and applied as specific biomarker lipids for such algae. We report here the presence of saturated C28, C30 and C32 1,14-diols in a culture of the marine heterokont alga Apedinella radians (Class Dictyochophyceae, order Pedinellales). Apedinella species occur globally, although predominantly in estuarine waters, so the finding has potential implications for the use of long chain 1,14-diols as biomarkers of Proboscia diatoms and as an indicator of upwelling.  相似文献   

3.
Long-chain alkyl diols contain an alkyl chain with alcohol groups at C1 and at the middle position of carbon chain, which exist widely in seas, rivers and lakes. It has been proven that these compounds are relatively resistant to degradation and have an extended occurrence in the geological record. In addition, they are relatively easy to identify. Therefore, long-chain alkyl diols can be used as potential biomarkers to trace the past change in paleoenvironment and paleoclimate. Although the sources of long-chain alkyl diols are still uncertain, the studies indicate that 1, 13 and 1, 15-diols are mainly produced by eustigmatophytes, while 14-diols are mainly from diatom Proboscia. So far, some proxies based on long-chain alkyl diols have been established to indicate the change in diatom productivity, upwelling intensity, salinity, sea surface temperature, riverine organic matter input and surface seawater nutrient concentration, which are significant for paleoenvironmental reconstruction. Current research and application of long-chain alkyl diols proxies were summarized, which would be helpful for further studying the source of long-chain alkyl diols and the application of relevant proxies in China’s marginal sea.  相似文献   

4.
长链烷基二醇类化合物(Long-chain alkyl diols)是指在碳链的1号位置和链中位置连接有羟基基团的类脂化合物,普遍存在于海洋、河流和湖泊环境中。由于这类化合物分布广泛、性质稳定不易降解、且检测手段较为简单,因此具有作为生物标志物的潜力,在生物地球化学领域引起了广泛的研究和关注。关于其生物来源尚未有定论,但是研究发现1,13-diols和1,15-diols可能主要来自真眼点藻,而14-diols主要来自硅藻Proboscia。目前根据长链烷基二醇建立的指标包括:硅藻生产力、上升流强度、盐度、温度、河流输入和表层海水营养盐浓度等,对古环境气候的重建有着重要的意义。归纳总结了目前长链烷基二醇指标的研究和应用进展,这有助于未来我国边缘海长链烷基二醇来源以及二醇指标的深入研究。  相似文献   

5.
Lipid biomarkers in lacustrine sediments provide valuable information about lake history and environmental change. Here we report the occurrence of a unique set of lipid biomarkers from a freshwater crater lake, El Junco, in the Galápagos. In addition to previously reported alkadienes, botryococcenes and lycopadienes indicative of Botryococcus braunii A, B and L races, we find highly branched C25 isoprenoids (HBIs) from diatoms, monomethyl alkanes likely from insect epicuticular waxes, long chain alkenols, diols and a triol, keto-ols, hydroxy acids and keto acids. Saturated and mono-unsaturated long chain diols from C30-C36 had terminal hydroxyl groups and hydroxyl groups between the ω16 and ω20 positions. Vicinal diols with hydroxyl groups at ω9 and ω10 were likely from the floating fern Azolla. C30-C36 keto-ols, mid-chain hydroxy and keto acids had mid-chain functional groups at similar positions to the diols, suggesting common origins. The predominance of ω20-hydroxy acids and diols, together with 20,21-dihydroxy-nonacosanoic acid is indicative of an Azolla source, while ω16 and ω18 hydroxy acids and diols imply a microalgal source.  相似文献   

6.
We have determined the accumulation rates and carbon isotopic compositions (δ13C) of long-chain (C24-C32) terrigenous plant wax fatty acids in 19 surface sediment samples geographically distributed throughout the Arabian Sea in order to assess the relationship between plant wax inputs and the surrounding monsoon wind systems. Both the accumulation rate data and the δ13C data show that there are three primary eolian sources of plant waxes to the Arabian Sea: Africa, Asia, and the Arabian Peninsula. These sources correspond to the three major wind systems in this region: the summer (Southwest) monsoon, the winter (Northeast) monsoon, and the summer northwesterlies that blow over the Arabian Peninsula. In addition, plant waxes are fluvially supplied to the Gulf of Oman and the Eastern African margin by nearby rivers. Plant wax δ13C values reflect the vegetation types of the continental source regions. Greater than 75% of the waxes from Africa and Asia are derived from C4 plants. Waxes delivered by northwesterly winds reflect a greater influence (25-40%) of C3 vegetation, likely derived from the Mesopotamian region. These data agree well with previously published studies of eolian dust deposition, particularly of dolomite derived from the Arabian Peninsula and the Mesopotamian region, in surface sediments of the Arabian Sea. The west-to-east gradient of plant wax δ13C and dolomite accumulation rates are separately useful indicators of the relationship between the northwesterly winds and the winds of the Southwest monsoon. Combined, however, these two proxies could provide a powerful tool for the reconstruction of both southwest monsoon strength as well as Mesopotamian aridity.  相似文献   

7.
Eocene sediments recovered from the Lomonosov Ridge in the central Arctic Ocean during Integrated Ocean Drilling Program Expedition 302 contain high amounts of fossil remains of the free floating freshwater fern Azolla. Both extant Azolla and the sediments from the Arctic Azolla interval were found to contain relatively high quantities of compounds identified as 1,ω20 C30–C36 diols. Furthermore, structurally related mid-chain hydroxy fatty acids, long chain n-alkanols and keto-ols were discovered. The different series have a common feature: there is always a hydroxy group at the ω20 position. In addition, structurally related C29 ω20,ω21 diols, C29 1,20,21 triols, C29 dihydroxy fatty acids as well as a series of wax esters containing these mono- and dihydroxy lipids are reported. Selective extraction of Azolla surface lipids revealed that these compounds are most likely present in the leaf waxes of the fern. The suite of long-chain, mid-chain ω20 hydroxy wax constituents is described for the first time. As they are well preserved in the Eocene sediments, these lipids may serve as palaeo-environmental indicators of the Arctic Azolla interval and as markers for the past occurrence of Azolla in general.  相似文献   

8.
A series of branched alkylbenzene ranging from C15 to C19 with several isomers (2–5) at each carbon number were identified in sediments from the Dongsheng sedimentary uranium ore deposits, Ordos Basin, China. The distribution patterns of the branched alkylbenzenes show significant differences in the sample extracts. The branched alkylbenzenes from organic-rich argillites and coals range from C15 to C19 homologues, in which the C17 or C18 dominated. On the other hand, the C19 branched alkylbenzenes dominated in the sandstone/siltstone extracts. The obvious differences of the branched alkylbenzene distributions between the uranium-host sandstones/siltstones and the interbedded barren organic-rich mudstones/coals probably indicate their potential use as biological markers associated with particular depositional environments and/or maturity diagenetic processes. Possible origins for these branched alkylbenzenes include interaction of simple aromatic compounds with, or cyclization and aromatization reactions of, these linear lipid precursors such as fatty acids, methyl alkanoates, wax esters or alkanes/alkenes that occur naturally in carbonaceous sediments. The possible simple aromatic compounds may include substituted benzenes, functionalized compounds such as phenols that are bound to kerogen at the benzyl position, and phenols that are decomposition products derived from aquatic and terrestrial sources. The distributions of methyl alkanoates and n-alkanes were found to be different between organic-rich mudstone/coal and sandstone/siltstone. From this result, it can be concluded that such differences of the alkylbenzene distributions were mainly resulting from the differences of organic precursors, although maturity effect and radiolytic alteration cannot be completely excluded.  相似文献   

9.
This paper reports on the spatial distribution patterns and investigates the controlling mechanisms of phytoplankton biomarkers (brassicasterol for diatoms, alkenones for haptophytes, dinosterol for dinoflagellates) and terrestrial biomarkers (odd C number long-chain (C27 + C29 + C31) n-alkanes) in surface sediments from the southern Yellow Sea (SYS). The contents of the phytoplankton biomarkers in the SYS surface sediments reveals a clear spatial pattern, with low values near the coasts and increased values seaward, caused by higher phytoplankton primary productivity and low sedimentation rates in the basin. The contents of terrestrial biomarkers show high values in the northern part of the study areas off the Shandong Peninsula and Jiangsu coast, caused by inputs of materials from the modern Huanghe River and the old Huanghe delta, respectively. The results also indicate that biomarker ratios offer the best approach for reconstructing marginal sea C cycles, as these proxies can be used to estimate the contributions of both terrestrial and marine organic matter and to reconstruct paleoproductivity and paleoecological changes in the SYS.  相似文献   

10.
Arabian Sea sediments record changes in the upwelling system off Arabia, which is driven by the monsoon circulation system over the NW Indian Ocean. In accordance with climate models, and differing from other large upwelling areas of the tropical ocean, a 500,000-yr record of productivity at ODP Site 723 shows consistently stronger upwelling during interglaciations than during glaciations. Sea-surface temperatures (SSTs) reconstructed from the alkenone unsaturation index (UK′37) are high (up to 27°C) during interglaciations and low (22-24°C) during glaciations, indicating a glacial-interglacial temperature change of >3°C in spite of the dampening effect of enhanced or weakened upwelling. The increased productivity is attributed to stronger monsoon winds during interglacial times relative to glacial times, whereas the difference in SSTs must be unrelated to upwelling and to the summer monsoon intensity. The winter (NE) monsoon was more effective in cooling the Arabian Sea during glaciations then it is now.  相似文献   

11.
The compositions of sterol, alcohol and ketone fractions from an oxic intertidal surface sediment from Corner Inlet. Victoria, Australia, have been examined by capillary gas chromatographymass spectrometry and related to the lipids of diatoms cultured from the sediment and to lipids of the sea-grass Zostera muelleri. Of the more than thirty sterols in the sediment most appear to derive from diatoms, including the major sterol 24-methylcholesta-5.22E-dien-3β-ol. Small amounts of 24-ethylcholesterol probably derive from Zostera, with a minor diatom contribution. 5α-stanols, both fully saturated and with a side-chain double bond, represented ca. 14% of the total sterols: a significant proportion of these are probably derived from marine invertebrates. These organisms also contribute C26 sterols. most of the cholesterol and possibly small amounts of Δ-sterols. The data suggest that in situ biohydrogenation of stenols was not a major process in sterol transformation in the surface oxic sediment. Alcohols ranged from C12 to C30 and showed an unusual abundance of unsaturated components with Δ9-16:1 being the major constituent. The long-chain alcohols probably originate largely from Zostera but the shorter-chain. C12-C20. alcohols are at least partly derived from wax esters of unknown origin. Diatoms do not contribute significant amounts of alcohols. Ketones were not major constituents of the sediment and consisted mainly of 6.10.14-trimethylpentadecan-2-one and a series of n-alkan-2-ones ranging from C16 to C33. The latter showed a similar distribution to that of the n-alkanes but the correspondence was not sufficient to substantiate a product-precursor relationship. Very long-chain C3- C39 unsaturated methyl and ethyl ketones, which may originate from the marine unicellular alga Emiliania huxleyi. were present in low concentration.  相似文献   

12.
Fatty acids (FAs), β- and ω-hydroxy acids, α,ω-dicarboxylic acids and n-alkanes were studied in a 200 m sediment core taken from Lake Biwa, Japan. FAs showed bimodal distribution with peaks at C16 and C22-C28. Their distribution patterns clearly changed with depth from lower molecular weight (C12-C19) predominance to higher molecular weight (C20-C32) predominance in the upper 20 m interval. Analyses of related compounds (β- and ω-hydroxy acids and α, ω-dicarboxylic acids) suggest that β- and ω-oxidative degradation of C12-C19 FAs has occurred in the sediments.The ratio of bound C12-C19 to unbound FAs increases with depth in the upper 0–1 m sediments, suggesting that unbound FAs are more labile. However, the ratio varies significantly in deeper sections and may be associated with water temperature.In the sediments deeper than 20 m in depth, C12-C19 FAs gradually decrease. On the other hand, higher molecular weight FAs (HFAs: C20-C32), which were probably derived from terrestrial plants, increase in concentration from 20 m to 100 m, suddenly decrease at 100 m and show progressively lower concentration in deeper sediments. These fluctuations are interpreted in relation to paleolimnological changes of the lake and the drainage basin. ω-Hydroxy C20-C30 acids and C20-C30α, ω-dicarboxylic acids show a distribution pattern similar to HFAs. Branched chain FAs, ω-hydroxy acids and C9-C19α,ω-dicarboxylic acids show a major peak around 3–15 m in depth. This peak is probably caused by increased bacterial activity in the water column and surface sediments in the past, which may be associated with an increase in primary production of the lake.  相似文献   

13.
Organic matter (OM) associated with the Dongsheng sedimentary U ore hosting sandstone/siltstone was characterized by Rock-Eval, gas chromatography–mass spectrometry and stable C isotope analysis and compared to other OM in the sandstone/siltstone interbedded organic matter-rich strata. The OM in all of the analyzed samples is Type III with Ro less than 0.6%, indicating that the OM associated with these U ore deposits can be classified as a poor hydrocarbon source potential for oil and gas. n-Alkanes in the organic-rich strata are characterized by a higher relative abundance of high-molecular-weight (HMW) homologues and are dominated by C25, C27 or C29 with distinct odd-to-even C number predominances from C23 to C29. In contrast, in the sandstone/siltstone samples, the n-alkanes have a higher relative abundance of medium-molecular-weight homologues and are dominated by C22 with no or only slight odd-to-even C number predominances from C23 to C29. Methyl alkanoates in the sandstone/siltstone extracts range from C14 to C30, maximizing at C16, with a strong even C number predominance, but in the organic-rich layers the HMW homologues are higher, maximizing at C24, C26 or C28, also with an even predominance above C22. n-Alkanes in the sandstone/siltstone sequence are significantly depleted in 13C relative to n-alkanes in most of the organic-rich strata. Diasterenes, ββ-hopanes and hopenes are present in nearly all the organic-rich sediments but in the sandstone/siltstone samples they occur as the geologically mature isomers. All the results indicate that the OM in the Dongsheng U ore body is derived from different kinds of source materials. The organic compounds in the organic-rich strata are mainly terrestrial, whereas, in the sand/siltstones, they are derived mainly from aquatic biota. Similar distribution patterns and consistent δ13C variations between n-alkanes and methyl alkanoates in corresponding samples suggest they are derived from the same precursors. The OM in the organic-rich strata does not appear to have a direct role in the precipitation of the U ore in the sandstone, but an indirect role cannot be excluded. The OM in the U hosting sandstone shows a relatively low hydrogen index, presumably due to oxidation or radiolytic damage.  相似文献   

14.
Biomarker accumulation rates in nine different time slices in three cores on and at the foot of a submarine high in the northern Arabian Sea (the Murray Ridge) were measured to investigate the influence of oxygen exposure time on the preservation of biomarker signals in the sedimentary record. All three sites experienced the same history of surface water productivity and sediment supply but had different bottom-water redox conditions due to their different positions (in, just below, well below) relative to the present location of the intense oxygen minimum zone (OMZ). Past variations in the intensity and position of the OMZ, known from a wide variety of proxies (TOC content, distribution and abundance of planktonic and benthic foraminifera and pteropods, trace metals, and δ15N), enabled specific biomarker (i.e., n-alkanes, steroids, alkenones, alkyldiols, C26 fatty acid, loliolide, biphytane diols, and archaeal tetraether lipids) accumulation rates at contrasting oxygen exposure times to be compared. The results indicate that these accumulation rates can vary by more than an order of magnitude for marine biomarkers. In addition, there are significant differences in the degree of oxic degradation of different types of biomarkers: Terrestrial n-alkanes are much more resistant than alkenones and n-alkyl diols, which are more refractory than steroids and biphytane diols. These differences in degree of oxic degradation indicate that biomarker distributions will change on increasing exposure to oxygen. These findings have a significant impact on the application of biomarkers to sedimentary settings in which oxygen exposure time is likely to change significantly.  相似文献   

15.
Hydroxy acids in sediments of Lakes Bonney, Fryxell, Joyce and Vanda, and unnamed ponds (B2, NF1, NF2 and L4) as well as in cyanobacterial mats from the McMurdo Sound region of southern Victoria Land in Antarctica have been studied to clarify their features and elucidate their source organisms. Normal and branched (iso and anteiso) 2-hydroxy acids were found in all the samples studied with the predominance of even- and odd-carbon numbers, respectively. The most dominant 2-hydroxy acids in the sediments were mainly short-chain components (<C20). Normal and branched 3-hydroxy acids were detectewith the predominance of even- and odd-carbon numbers, respectively, in total concentrations between 0.48 and 53 μg/g of dry sediment. (ω-1)-Hydroxy acids were all long-chains (C22, C24, C26, C28 and C30). 9,10-Dihydroxyhexadecanoic and/or 9,10-dihydroxyoctadecanoic acids were identified in all the sediments and a cyanobacterial mat. The composition of hydroxy acids differ considerably among the lakes and ponds, suggesting the difference of source organisms. These 2-, 3- and (ω-1)-hydroxy, and 9,10-dihydroxy acids may be derived from cyanobacteria and microalgae, in addition to non-photosynthetic microorganisms. Cyanobacteria and microalgae which are widely distributed in the world, may be important sources of hydroxy acids in the natural environments.  相似文献   

16.
The occurrence of long chain chloroalkenes and chloroalkanes has not been previously reported in natural sediments. Here we report the presence of long chain (C30–C36) n-chloroalkanes and chloroalkenes in the recent sediments of the only permanent freshwater lake in the Galápagos Islands, El Junco. Both chloroalkanes and chloroalkenes have a chlorine atom at the terminal position. The cis and trans alkenyl chlorides have double bonds near the middle of the hydrocarbon chain (ω15, 16, 17). Alkenes in the lake sediments are typically C23:1 to C27:1, substantially shorter than the chloroalkenes and chloroalkanes. The lipid chain lengths and the positions of functional groups imply a structural relationship between chloroalkenes and some alkenols, diols and (or) hydroxy acids that most likely derive from algae.  相似文献   

17.
Steryl alkyl ethers (SAEs) have been reported from marine sediments ranging from Holocene to Lower Cretaceous and their production has been linked to upwelling of cold, nutrient-rich water. However, the lack of continuous stratigraphic records for them has complicated validation of the precise connection of their production, sedimentary distribution and survival to climatic conditions. Here, we report an SAE record that spans the last ca. 135 ka from a core taken offshore southeastern Australia in the Murray Canyons Group region. The SAEs are composed predominantly of C27–C30 steroid moieties with one or two double bonds, ether-bound to C10–C11 alkyl moieties. Some of the SAEs are identical to those reported in marine sediments, whereas others have not been identified previously. They do not exhibit any systematic change in distribution over the past 110 ka but sediments older than 110 ka possess a different assemblage, with a higher amount of constituents containing a C11 alkyl moiety. The SAE accumulation rate increases rapidly during glacial episodes and for intervals characterized by a sharp decline in sea-surface temperature. The results suggest that SAEs may be related to marine eukaryotes that thrive when there is an influx of cold, deep waters in the Murray Canyons Group region, likely triggered by stronger westerlies over southeastern Australia forcing deeper water to reach the surface during glacials.  相似文献   

18.
The degradation of acyclic petroleum hydrocarbons was studied during a 24-month experiment in Mediterranean coastal sediments (Gulf of Fos). Sediment cores entirely contaminated with oil (Arabian Light Crude Oil) were incubated in situ. The use of conservative tracers of sediment's particles reworking (luminophores) allowed the distinction of the reworked layer from the anoxic deeper sediments. Using the 17α,21βC30 hopane (C30H) as an inert internal reference, we could demonstrate that, after 24 months of experiment, acyclic petroleum hydrocarbons can be degraded under natural anaerobic conditions. The reactivity of individual alkanes appeared to depend on their chemical structure. To cite this article: D. Massias et al., C. R. Geoscience 335 (2003).To cite this article: D. Massias et al., C. R. Geoscience 335 (2003).  相似文献   

19.
Two piston cores, one located far from the continents (The North Pacific Ocean: ES core), and another located comparatively closer to the continents (The Bering Sea: BOW-8a core) were investigated to reconstruct environmental changes on source land areas. The results show significant contribution of terrestrial organic matter to sediments in both cores. The δ13C values of n-C27, n-C29, and n-C31 alkanes in sediments from the North Pacific ES core show significant glacial to interglacial variation whereas those from the Bering Sea core do not. Variations of δ13C values of land plant n-alkanes are related to the environmental or vegetational changes in the source land areas. Environmental changes, especially, aridity, rainfall, and pCO2 during glacial/interglacial transitional periods can affect vegetation, and therefore C3 / C4 plant ratios, resulting in δ13C changes in the preserved land plant biomarkers. Maximum values of δ13C as well as maximum average chain length values of long chain n-alkanes in the ES core occur mostly at the interglacial to glacial transition zones reflecting a time lag related to incorporation of living organic matter into soil and transportation into ocean basins via wind and/or ability of C4 plants to adapt for a longer period before being replaced by C3 plants when subjected to gradual climatic changes. Irregular variations with no clear glacial to interglacial trends in the BOW-8a core may result from complex mixture of aerosols from westerly winds and riverine organic matter from the Bering Sea catchments. In addition, terrestrial organic matter entering the Bering Sea could originate from multiple pathways including eolian, riverine, and ice rafted debris, and possibly be disturbed by turbidity and other local currents which can induce re-suspension and re-sedimentation causing an obliterated time relation in the Bering Sea biomarker records.  相似文献   

20.
Ozokerite, a natural mixture of long-chain paraffins, is found at Ein-Humar (Jordan) on the eastern escarpment of the Dead Sea. The Ein-Humar ozokerite is mainly composed of saturated n-paraffins from C30 to presumably well into the C50′s with a maximum at C38. IR, NMR and chromatographic data indicate the absence of cycloparaffinic and aromatic molecules. The ozokerite is assumed to be related to the heavy asphalts and oils in the Dead Sea area. It probably forms by separation of high-molecular paraffins from non-paraffinaceous heavy oils or asphalts by geothermal heat and precipitation in the conduits due to lowering of temperature.  相似文献   

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